Sapphire 30 Special Order

Product NDC
48951-3191
11-digit product format
489513191
Labeler code
48951
Product ID
48951-3191_6b250584-d577-5166-e053-2991aa0af862
Type
HUMAN OTC DRUG
Nonproprietary name
Sapphire 30 Special Order
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
ALUMINUM OXIDE
Active strength
30 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-3191-32026-01-29C16284748780-149896155-a923-586f-e063-e6dba90add90Sapphire 30 Special Order

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3191-3Sapphire 30 Special Order60 mL in 1 BOTTLE, DROPPERLIQUID602

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALUMINUM OXIDEACTIVE INGREDIENTLMI26O6933SAPPHIRE 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
ALUMINUM OXIDEACTIVE MOIETYLMI26O6933SAPPHIRE 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RSAPPHIRE 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3191SAPPHIRE 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20180501_f9c489b8-f73d-4377-bfba-ba3555c6bbe3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3191-34895131910360 mL in 1 BOTTLE, DROPPER (48951-3191-3) 60 ml2009-09-010000-00-00NoNoCurrent